SKU: WR4182 Categories: ,

U-Blot® Rab7 Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR4182-50
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Product details

Background:RAB family members are small, RAS-related GTP-binding proteins that are important regulators of vesicular transport. Each RAB protein targets multiple proteins that act in exocytic / endocytic pathways. This gene encodes a RAB family member that regulates vesicle traffic in the late endosomes and also from late endosomes to lysosomes. This encoded protein is also involved in the cellular vacuolation of the VacA cytotoxin of Helicobacter pylori. Mutations at highly conserved amino acid residues in this gene have caused some forms of Charcot-Marie-Tooth (CMT) type 2 neuropathies. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetRAB7
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, ELISA
MW(Calculated)24kD
MW(Observed)24kD
Host SpeciesRabbit
IsotypeIgG,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000; WB 1:1000-1:5000; IF 1:200-1:1000; ELISA 1:5000-1:20000; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM0345R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameRAB7A RAB7
Protein NameRAB7A
Other Name
SpeciesHuman
Gene ID7879
UniprotP51149,
Species.1Mouse
Gene ID.119349
Uniprot.1P51150,
Species.2Rat
Gene ID.229448
Uniprot.2P09527
Cellular LocalizationCytoplasm
Tissue ExpressionWidely expressed; high expression found in skeletal muscle.
Signaling_pathwayCellular Processes >> Transport and catabolism >> Phagosome;Cellular Processes >> Transport and catabolism >> Autophagy - animal;Cellular Processes >> Transport and catabolism >> Mitophagy - animal
Research Areas>>Mitophagy - animal; / >>Autophagy - animal; / >>Endocytosis; / >>Phagosome; / >>Salmonella infection; / >>Amoebiasis; / >>Tuberculosis
FunctionDisease:Defects in RAB7A are the cause of Charcot-Marie-Tooth disease type 2B (CMT2B) [MIM:600882]; also known as hereditary motor and sensory neuropathy II (HMSN2). CMT2B is a form of Charcot-Marie-Tooth disease, the most common inherited disorder of the peripheral nervous system. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathy or CMT1, and primary peripheral axonal neuropathy or CMT2. Neuropathies of the CMT2 group are characterized by signs of axonal regeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy. CMT2B is clinically characterized by marked distal muscle weakness and a high frequency of foot ulcers, infections and amputations of the toes. CMT2B inheritance is autosomal dominant.,Function:Involved in late endocytic transport. Contributes to the maturation of phagosomes (acidification).,sequence Caution:Wrong choice of frame.,similarity:Belongs to the small GTPase superfamily. Rab family.,subcellular location:Identified by mass spectrometry in melanosome fractions from stage I to stage IV.,subunit:Interacts with RILP.,tissue specificity:Widely expressed; high expression found in skeletal muscle.,
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